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Crystal structure of the pmftn variant E44H soaked in iron (3 H)

Analyse Crystal structure of the pmftn variant E44H soaked in iron (3 H) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4ZL6
Type
protein
Length
947 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ferritin
EC
1.16.3.1
UniProt
B6DMH6
Ligands
FE
Pockets
9 · best druggability 0.55

Structure

x-ray diffraction · 3 distinct chains · 79% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B, C, D, EFerritin (EC 1.16.3.1)protein15880% helix, 1% strandB6DMH6
AFerritin (EC 1.16.3.1)protein15779% helix, 1% strandB6DMH6
FFerritin (EC 1.16.3.1)protein15878% helix, 1% strandB6DMH6

Ligands and binding sites

  • FE · Fe (III) ion · metal · 24 copies · chains B, A, C, D, E, F

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11620.550.8019empty
21190.530.8217empty
31040.480.8014empty
41050.450.7814empty
5890.410.7713empty

Interfaces

8 interfaces between chains.

  • D–E · 1025 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 1014 Ų buried · 6 hydrogen bonds · protein-protein
  • A–F · 994 Ų buried · 5 hydrogen bonds · protein-protein
  • A–E · 513 Ų buried · 6 hydrogen bonds · protein-protein
  • C–E · 501 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified (alkylation).

Compared structures

  • 4ZL6 · Crystal structure of the PmFTN variant E44H soaked in iron (3 h) · the same entry in another collection · chain B against B, TM-score 1.00

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